hyperprolinemia - caused by mutations in the ALDH4A1 gene Researchers have identified three mutations in the ALDH4A1 gene that eliminate the function of the pyrroline-5-carboxylate dehydrogenase enzyme, causing hyperprolinemia type II.
Hyperprolinemia Type I Causes, Symptoms And Treatment And Related Disorders
Two types of hyperprolinemia are recognized by physicians and clinical researchers. Each represents an inherited inborn error of metabolism involving the amino acid, proline.
Hyperprolinemia Type I
Hyperprolinemia Type II
Hyperpyrexia
HyperRHO S/D Full Dose - Medication
HyperRHO S/D Mini Dose - Medication
Hypersensitivity Pneumonitis
Hypersensitivity Vasculitis
Hypersplenism ...
Hyperprolinemia Type I
Hyperprolinemia Type II
Hyperpyrexia
Hypersensitivity Pneumonitis
Hypersensitivity Vasculitis
Hypersplenism
Hypertelorism with Esophageal Abnormalities and Hypospadias
Hypertelorism-Hypospadias Syndrome ...
deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency/translocase deficiency, Citrullinemia, Argininosuccinic aciduria, Argininemia, Hyperammonemia) - Glutaric acidemia type 1, type 2 - Hyperprolinemia - ...
 See also: Deficiency, Symptom, Inborn error of metabolism, Histidinemia, Alkaptonuria
  
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